Evidence map›Paper›PMID 35092315›Full record

ArticleHepatology (Baltimore, Md.)2022

Contrast-enhanced CT and liver surface nodularity for the diagnosis of porto-sinusoidal vascular disorder: A case-control study.

Shantha Ram Valainathan, Riccardo Sartoris, Laure Elkrief, Marta Magaz, Fabian Betancourt, Silvia Pellegrino, Arianna Nivolli, Marco Dioguardi Burgio, Yves Flattet, Sylvain Terraz and 13 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Hepatology (Baltimore, Md.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Elevated Hepatic Copper Content in Porto-Sinusoidal Vascular Disorder (PSVD): Leading Down a Wrong Track.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
  7. Article
  8. Imaging in Vascular Liver Diseases.Medicina (Kaunas, Lithuania) · 2024
    Review
  9. Review
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 6 institutions in 4 countries.

Shantha Ram ValainathanService d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, Centre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, AP-HP, Hôpital Beaujon, Paris, France.ORCID 0000-0002-9980-2104
Riccardo SartorisCentre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, Paris, France.
Laure ElkriefService d'Hépato-gastroentérologie, Hôpitaux Universitaires de Genève, Geneva, Switzerland.ORCID 0000-0003-2843-1710
Marta MagazBarcelona Hepatic Hemodynamic Laboratory, Liver Unit, Hospital Clínic de Barcelona, IDIBAPS, CIBERehd, European Reference Network for Rare Vascular Liver Diseases, Universitat de Barcelona, Barcelona, Spain.
Fabian BetancourtBarcelona Hepatic Hemodynamic Laboratory, Liver Unit, Hospital Clínic de Barcelona, IDIBAPS, CIBERehd, European Reference Network for Rare Vascular Liver Diseases, Universitat de Barcelona, Barcelona, Spain.
Silvia PellegrinoCentre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, Paris, France.
Arianna NivolliCentre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, Paris, France.
Marco Dioguardi BurgioCentre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, Paris, France.
Yves FlattetService d'Hépato-gastroentérologie, Hôpitaux Universitaires de Genève, Geneva, Switzerland.
Sylvain TerrazDepartment of Radiology, University Hospitals of Geneva, Geneva, Switzerland.
Nicolas DrilhonService d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, Centre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, AP-HP, Hôpital Beaujon, Paris, France.
Marie LazarethService d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, Centre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, AP-HP, Hôpital Beaujon, Paris, France.
Julia HerrouDepartment of Rhumatology, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, Paris, France.
Onorina BrunoCentre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, Paris, France.
Audrey PayanceService d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, Centre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, AP-HP, Hôpital Beaujon, Paris, France.
Aurélie PlessierService d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, Centre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, AP-HP, Hôpital Beaujon, Paris, France.ORCID 0000-0001-5656-1622
François DurandService d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, Centre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, AP-HP, Hôpital Beaujon, Paris, France.
Maxime RonotCentre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, Paris, France.ORCID 0000-0001-7464-3939
Dominique-Charles VallaService d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, Centre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, AP-HP, Hôpital Beaujon, Paris, France.
Valérie ParadisDepartment of Pathology, Université de Paris, AP-HP, Hôpital Beaujon, Beaujon Hospital, Assistance Publique-Hôpitaux de Paris, Clichy, France.
Juan Carlos Garcia-PaganBarcelona Hepatic Hemodynamic Laboratory, Liver Unit, Hospital Clínic de Barcelona, IDIBAPS, CIBERehd, European Reference Network for Rare Vascular Liver Diseases, Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0001-9032-4954
Valérie VilgrainCentre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, Paris, France.
Pierre-Emmanuel RautouService d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, Centre de Recherche sur l'inflammation, Inserm, UMR 1149, Université de Paris, AP-HP, Hôpital Beaujon, Paris, France.ORCID 0000-0001-9567-1859
Inserm · FRHospital Clínic de Barcelona · ESHôpital Beau-Séjour · CHHôpital Beaujon · FRHôpital Cochin · FRUniversity Hospital of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsPorto-sinusoidal vascular disorder (PSVD) is a rare and commonly overlooked cause of portal hypertension. The interest of CT analysis, including quantification of liver surface nodularity (LSN) for PSVD diagnosis has not been established. This study aimed at assessing the performance of LSN and CT features for a PSVD diagnosis in patients with signs of portal hypertension. APPROACH AND

resultsThis retrospective case-control study included a learning cohort consisting of 50 patients with histologically proven PSVD, according to VALDIG criteria, and 100 control patients with histologically proven cirrhosis, matched on ascites. All patients and controls had at least one sign of portal hypertension and CT available within 1 year of liver biopsy. Principal component analysis of CT features separated patients with PSVD from patients with cirrhosis. Patients with PSVD had lower median LSN than those with cirrhosis (2.4 vs. 3.1, p < 0.001). Multivariate analysis identified LSN < 2.5 and normal-sized or enlarged segment IV as independently associated with PSVD. Combination of these two features had a specificity of 90% for PSVD and a diagnostic accuracy of 84%. Even better results were obtained in an independent multicenter validation cohort including 53 patients with PSVD and 106 control patients with cirrhosis (specificity 94%, diagnostic accuracy 87%).

conclusionsThis study that included a total of 103 patients with PSVD and 206 patients with cirrhosis demonstrates that LSN < 2.5 combined with normal-sized or enlarged segment IV strongly suggests PSVD in patients with signs of portal hypertension.

Indexed as

Hypertension, PortalVascular DiseasesCase-Control StudiesFibrosisHumansLiverLiver CirrhosisRetrospective StudiesTomography, X-Ray Computed

Identifiers

PMID35092315
PMCPMC9544289
OpenAlexW4210703681

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.